Director of Quality & Regulatory Affairs — ISO 13485 Lead

A boutique medical device company in Miami is seeking a Quality & Regulatory Affairs Director to lead quality operations and regulatory compliance. The role demands maintaining ISO 13485 Quality Management System and ensuring audit readiness. The ideal candidate will be an experienced leader from a medical device manufacturing background, who is hands-on and thrives in a collaborative small team environment. This opportunity offers high visibility working closely with executive leadership and shaping quality processes. #J-18808-Ljbffr